Canonical Allele Identifier: CA3154042
Gene: CASP3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2705897

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184631944T>G , CM000666.2:g.184631944T>G GRCh38
NC_000004.11:g.185553098T>G , CM000666.1:g.185553098T>G GRCh37
NC_000004.10:g.185790092T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_004346.3:c.308-4A>C VV NP_004337.2:p.=
NM_032991.2:c.308-4A>C VV NP_116786.1:p.=
XM_011532301.1:c.308-4A>C XP_011530603.1:p.=
NM_001354777.1:c.308-4A>C VV NP_001341706.1:p.=
NM_001354779.1:c.230-4A>C VV NP_001341708.1:p.=
NM_001354780.1:c.230-4A>C VV NP_001341709.1:p.=
NM_001354781.1:c.308-4A>C VV NP_001341710.1:p.=
NM_001354782.1:c.308-4A>C VV NP_001341711.1:p.=
NM_001354783.1:c.335-4A>C VV NP_001341712.1:p.=
NM_001354784.1:c.230-4A>C VV NP_001341713.1:p.=
NM_004346.4:c.308-4A>C VV MANE Preferred NP_004337.2:p.=
ENST00000308394.8:c.308-4A>C ENSP00000311032.4:p.=
ENST00000393585.6:c.308-4A>C ENSP00000377210.2:p.=
ENST00000393588.8:c.308-4A>C ENSP00000377213.4:p.=
ENST00000447121.2:c.308-4A>C ENSP00000407142.2:p.=
ENST00000517513.5:c.308-4A>C ENSP00000428372.1:p.=
ENST00000523916.5:c.308-4A>C ENSP00000428929.1:p.=
ENST00000613118.4:c.335-4A>C ENSP00000478339.1:p.=